US4111793A - Olefins production - Google Patents
Olefins production Download PDFInfo
- Publication number
- US4111793A US4111793A US05/722,552 US72255276A US4111793A US 4111793 A US4111793 A US 4111793A US 72255276 A US72255276 A US 72255276A US 4111793 A US4111793 A US 4111793A
- Authority
- US
- United States
- Prior art keywords
- catalyst
- process according
- steam
- manganese
- bed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 150000001336 alkenes Chemical class 0.000 title claims abstract description 9
- 239000003054 catalyst Substances 0.000 claims abstract description 33
- 238000000034 method Methods 0.000 claims abstract description 14
- 238000005336 cracking Methods 0.000 claims abstract description 6
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 4
- 239000011572 manganese Substances 0.000 claims abstract description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 18
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 18
- 229930195733 hydrocarbon Natural products 0.000 claims description 17
- 150000002430 hydrocarbons Chemical class 0.000 claims description 17
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 15
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 238000009835 boiling Methods 0.000 claims description 7
- 150000002697 manganese compounds Chemical class 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 claims 6
- 230000005484 gravity Effects 0.000 claims 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 239000012263 liquid product Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- 238000004230 steam cracking Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- -1 manganese nitrate Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/32—Manganese, technetium or rhenium
- B01J23/34—Manganese
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/02—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils characterised by the catalyst used
- C10G11/04—Oxides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/10—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with stationary catalyst bed
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/14—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
- C10G11/18—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/20—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert heated gases or vapours
Definitions
- the present invention relates to a method of producing olefins by catalytic cracking of high boiling hydrocarbon feedstock.
- Low molecular weight olefins such as ethylene and propylene
- olefins have been produced from low boiling hydrocarbons feedstock by thermal cracking at temperatures between 500° and 1,000° C.
- Hydrocarbon feedstocks which have been converted to olefins in this manner range from those containing lower paraffinic hydrocarbons such as naphtha boiling up to about 200° C and gas oils boiling above this range up to 350° C, to wax distillates boiling between 300° and 550° C.
- the manganese compound is preferably manganese dioxide although other manganese compounds may be envisaged.
- the manganese compound is suitably supported on a refractory oxide such as zirconia, titania, silica or alumina although zirconia and titania are preferred as supports.
- the catalyst is prepared by impregnating the support with a soluble manganese compound such as manganese nitrate, followed by heating to convert the nitrate to the oxide.
- the supported catalyst suitably contains between 1 and 20%, preferably between 5 and 15% by weight of manganese.
- the catalyst may either be in the form of a fixed or a fluidised bed.
- the catalyst in the reactor is suitably maintained at a temperature between 650° and 900° C, preferably below 870° at the time of cracking.
- the mixing of steam and hydrocarbon may be achieved either by introducing them pre-mixed into the reactor tubes containing the catalyst for fixed bed operations or they may be introduced separately but simultaneously for fluid bed operations either in parallel or in counter current fashion onto the catalyst bed.
- the hydrocarbon and steam are pre-mixed, they are preferably pre-heated to a temperature of about 450°-550° C at the inlet of the catalyst tubes.
- the weight ratio of steam to hydrocarbon would depend upon the nature of the hydrocarbon but for wax distillate it is preferably between 1:1 and 2:1.
- the steam cracking may be carried out at atmospheric or super atmospheric pressures.
- the MnO 2 /TiO 2 and MnO 2 /ZrO 2 catalysts were used to test the cracking of wax distillate in a fixed bed.
- the steam cracking was carried out by placing MnO 2 /TiO 2 (75g) catalyst charge in the body of a quartz bed reactor and partially fluidising the bed with steam, which was preheated to between 800° and 1000° C and then passed up through a sintered distributor plate. Kuwait wax distillate (1 ml./min) was dropped vertically onto the fluidised catalyst bed controlling the temperature of the hydrocarbon at its injection point between 250° and 300° C by adjusting the nozzle injection position relative to the catalyst bed. After 1 hour a sample of the reaction products was taken and analysed (Table 3).
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
This invention relates to a method of producing olefins from a wax distillate feed by cracking the feed in the presence of steam at a catalyst temperature of between 650° and 900° C over a manganese catalyst.
Description
The present invention relates to a method of producing olefins by catalytic cracking of high boiling hydrocarbon feedstock.
Low molecular weight olefins, such as ethylene and propylene, are very useful raw material for the chemical inudstry. Conventionally, such olefins have been produced from low boiling hydrocarbons feedstock by thermal cracking at temperatures between 500° and 1,000° C. Hydrocarbon feedstocks which have been converted to olefins in this manner range from those containing lower paraffinic hydrocarbons such as naphtha boiling up to about 200° C and gas oils boiling above this range up to 350° C, to wax distillates boiling between 300° and 550° C.
It has now been found that by using a suitable catalyst in a fixed bed process the yield of the desired olefins from wax distillates can be improved.
Accordingly, the present invention is a process for producing olefins by cracking at elevated temperature in the presence of steam a hydrocarbon feedstock consisting essentially of wax distillate and boiling between 300°-550° C over a catalyst comprising a compound of manganese.
The manganese compound is preferably manganese dioxide although other manganese compounds may be envisaged. The manganese compound is suitably supported on a refractory oxide such as zirconia, titania, silica or alumina although zirconia and titania are preferred as supports. The catalyst is prepared by impregnating the support with a soluble manganese compound such as manganese nitrate, followed by heating to convert the nitrate to the oxide. The supported catalyst suitably contains between 1 and 20%, preferably between 5 and 15% by weight of manganese.
The catalyst may either be in the form of a fixed or a fluidised bed. The catalyst in the reactor is suitably maintained at a temperature between 650° and 900° C, preferably below 870° at the time of cracking.
The mixing of steam and hydrocarbon may be achieved either by introducing them pre-mixed into the reactor tubes containing the catalyst for fixed bed operations or they may be introduced separately but simultaneously for fluid bed operations either in parallel or in counter current fashion onto the catalyst bed. Where the hydrocarbon and steam are pre-mixed, they are preferably pre-heated to a temperature of about 450°-550° C at the inlet of the catalyst tubes.
The weight ratio of steam to hydrocarbon would depend upon the nature of the hydrocarbon but for wax distillate it is preferably between 1:1 and 2:1.
The steam cracking may be carried out at atmospheric or super atmospheric pressures.
The invention is further illustrated with reference to the following Examples.
MnO2 /TiO2
136g manganese nitrate solution (50% w/w solution as Mn(NO3)2, 6H2 O) were added to 206g titanium dioxide and 150 ml. distilled water to form a white slurry. The slurry was evaporated to dryness over a hot plate, then finally oven dried at 120° C. The catalyst was then heated at 400° C for 2 hours to decompose the nitrate to the oxide, and finally for a further 2 hours at 600° C. The catalyst was broken down to between BSS mesh 25-60 for use in the fluid bed.
MnO2 /ZrO2
66g manganese nitrate solution (50% w/w solution as Mn(NO3)2, 6H2 O) was added to 90g zirconium dioxide pellets. The mixture was evaporated to dryness over a steam bath and then dried overnight at 120° C. The catalyst was heated to 600° C in air overnight before use.
Steam Cracking
The MnO2 /TiO2 and MnO2 /ZrO2 catalysts were used to test the cracking of wax distillate in a fixed bed.
15g MnO2 /TiO2 catalyst occupying about 18 ml. was charged to a quartz reactor. Kuwait wax distillate (1 ml./min) and steam (generated from water pumped at 1 ml./min) were passed over the catalyst for 2 hours at a maximum reactor temperature maintained at 860° C. Analysis at the major reaction products is given in Table 1.
Table 1
______________________________________
Catalyst 9% MnO.sub.2 /TiO.sub.2
Reactor Fixed bed
Steam hydrocarbon wt.ratio
1.0:1.0
Products (% wt on feed)
Hydrogen 1.1
Methane 11.4
Ethylene 20.1
Ethane 1.9
Propylene 7.1
Butadiene 3.0
Other C.sub.4 's 2.1
C.sub.5 + liquid products
45.0
CO.sub.2 1.2
______________________________________
32g MnO2 /ZrO2 occupying 18 ml. were packed into a quartz reactor. Kuwait wax distillate (1 ml./min) and steam (generated from water pumped at 1 ml./min) were passed over the catalyst for 2 hours at a maximum reactor temperature maintained at 827° C. Analysis of major reaction products is given in Table 2.
TABLE 2
______________________________________
Catalyst 10% MnO.sub.2 /ZrO.sub.2
Reactor Fixed Bed
Steam:Hydrocarbon wt.ratio
1.0:1.0
Products (% wt on feed)
Hydrogen 1.0
Methane 8.0
Ethylene 23.3
Ethane 2.0
Propylene 10.0
Butadiene 4.8
Other C.sub.4 's 2.5
C.sub.5 + liquid products
37.5
CO.sub.2 2.1
______________________________________
The steam cracking was carried out by placing MnO2 /TiO2 (75g) catalyst charge in the body of a quartz bed reactor and partially fluidising the bed with steam, which was preheated to between 800° and 1000° C and then passed up through a sintered distributor plate. Kuwait wax distillate (1 ml./min) was dropped vertically onto the fluidised catalyst bed controlling the temperature of the hydrocarbon at its injection point between 250° and 300° C by adjusting the nozzle injection position relative to the catalyst bed. After 1 hour a sample of the reaction products was taken and analysed (Table 3).
Table 3
______________________________________
Catalyst 9% MnO.sub.2 /TiO.sub.2
Reactor Moving bed
Steam hydrocarbon wt.ratio
1.1:1.0
Products (% wt on feed)
Hydrogen 1.4
Methane 11.9
Ethylene 16.6
Ethane 2.6
Propylene 7.6
Butadiene 2.2
Other C.sub.4 's 2.0
C.sub.5 + liquid products
54.1
CO 0.1
CO.sub.2 7.7
______________________________________
Claims (10)
1. A process of producing olefins by cracking at elevated temperature in the presence of steam a hydrocarbon feedstock consisting essentially of wax distillate and boiling between 300° and 550° C over a catalyst composition consisting essentially of a manganese oxide and zirconia or titania.
2. A process according to claim 1 wherein the manganese compound is manganese dioxide.
3. A process according to claim 1 wherein the catalyst contains between 1 and 20% by weight of manganese.
4. A process according to claim 1 wherein the catalyst is maintained as a fixed bed.
5. A process according to claim 1 wherein the catalyst is maintained as a fluidised bed.
6. A process according to claim 5 wherein the cracking is carried out by bringing the steam and hydrocarbon feedstock into contact with the catalyst bed from substantially opposite directions.
7. A process according to claim 6 wherein the hydrocarbon feedstock is brought into contact with the catalyst bed under force of gravity.
8. A process according to claim 1 wherein the steam and hydrocarbons are premixed and preheated prior to contact with the catalyst.
9. A process as defined in claim 1 wherein said catalyst composition consists essentially of a manganese oxide and zirconia.
10. A process as defined in claim 1 wherein said catalyst composition consists essentially of a manganese oxide and titania.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB39284/75 | 1975-09-25 | ||
| GB39284/75A GB1492880A (en) | 1975-09-25 | 1975-09-25 | Olefins production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4111793A true US4111793A (en) | 1978-09-05 |
Family
ID=10408733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/722,552 Expired - Lifetime US4111793A (en) | 1975-09-25 | 1976-09-13 | Olefins production |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4111793A (en) |
| JP (1) | JPS5239604A (en) |
| BE (1) | BE846507A (en) |
| CA (1) | CA1077067A (en) |
| DE (1) | DE2641455A1 (en) |
| FR (1) | FR2325711A1 (en) |
| GB (1) | GB1492880A (en) |
| IT (1) | IT1070567B (en) |
| NL (1) | NL7610632A (en) |
Cited By (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4200609A (en) * | 1978-04-03 | 1980-04-29 | Mcdonnell Douglas Corporation | Ozone removal filter containing manganese dioxide and ceric oxide catalysts |
| US4207291A (en) * | 1978-04-03 | 1980-06-10 | Mcdonnell Douglas Corporation | Ozone removal filter having manganese dioxide coated thereon |
| US4952381A (en) * | 1986-07-25 | 1990-08-28 | Sakai Chemical Industry Co., Ltd. | Method for denitrizing nitrogen oxides contained in waste gas |
| US5380690A (en) * | 1993-03-29 | 1995-01-10 | China Petro-Chemical Corporation | Cracking catalyst for the production of light olefins |
| US5670037A (en) * | 1993-11-05 | 1997-09-23 | China Petro-Chemical Corporation | Process for producing light olefins by catalytic conversion of hydrocarbons |
| US6497812B1 (en) * | 1999-12-22 | 2002-12-24 | Chevron U.S.A. Inc. | Conversion of C1-C3 alkanes and fischer-tropsch products to normal alpha olefins and other liquid hydrocarbons |
| US20050080308A1 (en) * | 2002-08-19 | 2005-04-14 | Sang-Mun Jeong | Hydrocarbon steam cracking catalyst for olefin preparation, method for preparing the same, and olefin preparation method using the same |
| US20060084568A1 (en) * | 2004-10-18 | 2006-04-20 | Filimonov Igor N | Hydrocarbon cracking catalyst using chemical liquid depositon and method for preparing the same |
| US20060116544A1 (en) * | 2002-10-28 | 2006-06-01 | Idemitsu Kosan Co., Ltd. | Process for producing olefin by catalytic cracking of hydrocarbon |
| US20060178546A1 (en) * | 2004-08-10 | 2006-08-10 | Weijian Mo | Method and apparatus for making a middle distillate product and lower olefins from a hydrocarbon feedstock |
| US20060191820A1 (en) * | 2004-08-10 | 2006-08-31 | Weijian Mo | Hydrocarbon cracking process for converting gas oil preferentially to middle distillate and lower olefins |
| US20070170093A1 (en) * | 2004-04-22 | 2007-07-26 | Sang-Mun Jeong | Hydrocarbon cracking catalyst and method for preparing the same |
| CN100392047C (en) * | 2005-06-09 | 2008-06-04 | 中国科学院大连化学物理研究所 | A method for producing olefins by catalytic oxidation cracking of petroleum hydrocarbons |
| US20090012340A1 (en) * | 2007-07-05 | 2009-01-08 | Lg Chem, Ltd. | Thermal-cracking method of hydrocarbon |
| US20090105066A1 (en) * | 2007-05-25 | 2009-04-23 | Lg Chem, Ltd. | Catalyst for hydrocarbon steam cracking, method of preparing the same and method of preparing olefin by using the same |
| US20100133146A1 (en) * | 2008-12-02 | 2010-06-03 | Van Egmond Cor Franciscus | Coil for pyrolysis heater and method of cracking |
| US20100163455A1 (en) * | 2007-04-13 | 2010-07-01 | Hadjigeorge George A | Systems and methods for making a middle distillate product and lower olefins from a hydrocarbon feedstock |
| US20100200460A1 (en) * | 2007-04-30 | 2010-08-12 | Shell Oil Company | Systems and methods for making a middle distillate product and lower olefins from a hydrocarbon feedstock |
| US20100312032A1 (en) * | 2009-06-08 | 2010-12-09 | Lg Chem, Ltd. | Catalyst for hydrocarbon steam cracking, method of preparing the same and method of preparing olefin by using the same |
| US20100324232A1 (en) * | 2007-10-10 | 2010-12-23 | Weijian Mo | Systems and methods for making a middle distillate product and lower olefins from a hydrocarbon feedstock |
| US11851622B1 (en) | 2022-07-15 | 2023-12-26 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a gasification unit and steam enhanced catalytic cracker |
| US20240018433A1 (en) * | 2022-07-15 | 2024-01-18 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a delayed coker, steam enhanced catalytic cracker, and an aromatics complex |
| US20240018432A1 (en) * | 2022-07-15 | 2024-01-18 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a gasification unit, steam enhanced catalytic cracker, and an aromatics complex |
| US11939541B2 (en) | 2022-07-15 | 2024-03-26 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a delayed coker, steam enhanced catalytic cracker, and an aromatics complex |
| US12227709B2 (en) * | 2022-07-15 | 2025-02-18 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a gasification unit, dehydrogenation unit, steam enhanced catalytic cracker, and an aromatics complex |
| US12241029B2 (en) | 2022-07-15 | 2025-03-04 | Saudi Arabian Oil Company | Process for the conversion of petroleum to light olefins utilizing a pretreatment complex and steam enhanced catalytic cracker |
| US12325834B2 (en) | 2022-07-15 | 2025-06-10 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a delayed coker and steam enhanced catalytic cracker |
| US12325833B2 (en) | 2022-07-15 | 2025-06-10 | Saudi Arabian Oil Company | Methods for processing a hydrocarbon oil feed stream utilizing a delayed coker and steam enhanced catalytic cracker |
| US12391890B2 (en) * | 2020-09-01 | 2025-08-19 | Saudi Arabian Oil Company | Integrated process for conversion of whole crude to light olefins |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4621162A (en) * | 1985-07-25 | 1986-11-04 | Phillips Petroleum Company | Method for conversion of C3 and C4 hydrocarbons to olefinic products |
| US4579997A (en) * | 1985-07-25 | 1986-04-01 | Phillips Petroleum Company | Olefin production over catalytic oxides of Mn and at least one of Nb and a lanthanide |
| DE69021267T2 (en) * | 1989-05-11 | 1995-12-21 | Nippon Catalytic Chem Ind | Process for purifying a gas using an electrically heated MnO2 catalyst. |
| TW209182B (en) * | 1990-09-29 | 1993-07-11 | Catalyst co ltd | |
| JP6301705B2 (en) * | 2014-03-28 | 2018-03-28 | 日立造船株式会社 | Method for supporting manganese dioxide and method for producing porous ceramic member |
| US20220017829A1 (en) * | 2020-07-20 | 2022-01-20 | Saudi Arabian Oil Company | Systems and processes for direct converting distillate fractions of crude oil to olefins |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2611789A (en) * | 1949-10-17 | 1952-09-23 | Shell Dev | Production of alpha olefins |
| US3541179A (en) * | 1966-11-10 | 1970-11-17 | Japan Gasoline | Process for manufacturing olefins by catalytic partial oxidation of hydrocarbons |
| US3575848A (en) * | 1967-02-13 | 1971-04-20 | Mobil Oil Corp | Natural maganese oxide minerals as hydrocarbon conversion catalysts |
| US3647682A (en) * | 1968-10-23 | 1972-03-07 | Union Carbide Corp | Olefin production by the catalytic treatment of hydrocarbons |
| US3725495A (en) * | 1969-12-23 | 1973-04-03 | Toksoe H | Catalytic steam cracking of hydrocarbons and catalysts therefor |
| US3781195A (en) * | 1971-01-06 | 1973-12-25 | Bp Chem Int Ltd | Process for the production of gaseous olefins from petroleum distillate feedstocks |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1603110A (en) * | 1968-06-25 | 1971-03-22 |
-
1975
- 1975-09-25 GB GB39284/75A patent/GB1492880A/en not_active Expired
-
1976
- 1976-09-13 US US05/722,552 patent/US4111793A/en not_active Expired - Lifetime
- 1976-09-15 DE DE19762641455 patent/DE2641455A1/en not_active Ceased
- 1976-09-15 CA CA261,313A patent/CA1077067A/en not_active Expired
- 1976-09-22 IT IT27516/76A patent/IT1070567B/en active
- 1976-09-23 BE BE170881A patent/BE846507A/en unknown
- 1976-09-24 NL NL7610632A patent/NL7610632A/en not_active Application Discontinuation
- 1976-09-24 FR FR7628720A patent/FR2325711A1/en active Granted
- 1976-09-25 JP JP51115337A patent/JPS5239604A/en active Pending
Patent Citations (6)
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| US2611789A (en) * | 1949-10-17 | 1952-09-23 | Shell Dev | Production of alpha olefins |
| US3541179A (en) * | 1966-11-10 | 1970-11-17 | Japan Gasoline | Process for manufacturing olefins by catalytic partial oxidation of hydrocarbons |
| US3575848A (en) * | 1967-02-13 | 1971-04-20 | Mobil Oil Corp | Natural maganese oxide minerals as hydrocarbon conversion catalysts |
| US3647682A (en) * | 1968-10-23 | 1972-03-07 | Union Carbide Corp | Olefin production by the catalytic treatment of hydrocarbons |
| US3725495A (en) * | 1969-12-23 | 1973-04-03 | Toksoe H | Catalytic steam cracking of hydrocarbons and catalysts therefor |
| US3781195A (en) * | 1971-01-06 | 1973-12-25 | Bp Chem Int Ltd | Process for the production of gaseous olefins from petroleum distillate feedstocks |
Cited By (48)
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| US4200609A (en) * | 1978-04-03 | 1980-04-29 | Mcdonnell Douglas Corporation | Ozone removal filter containing manganese dioxide and ceric oxide catalysts |
| US4207291A (en) * | 1978-04-03 | 1980-06-10 | Mcdonnell Douglas Corporation | Ozone removal filter having manganese dioxide coated thereon |
| US4952381A (en) * | 1986-07-25 | 1990-08-28 | Sakai Chemical Industry Co., Ltd. | Method for denitrizing nitrogen oxides contained in waste gas |
| US5380690A (en) * | 1993-03-29 | 1995-01-10 | China Petro-Chemical Corporation | Cracking catalyst for the production of light olefins |
| US5670037A (en) * | 1993-11-05 | 1997-09-23 | China Petro-Chemical Corporation | Process for producing light olefins by catalytic conversion of hydrocarbons |
| US6497812B1 (en) * | 1999-12-22 | 2002-12-24 | Chevron U.S.A. Inc. | Conversion of C1-C3 alkanes and fischer-tropsch products to normal alpha olefins and other liquid hydrocarbons |
| US20050080308A1 (en) * | 2002-08-19 | 2005-04-14 | Sang-Mun Jeong | Hydrocarbon steam cracking catalyst for olefin preparation, method for preparing the same, and olefin preparation method using the same |
| US20060058563A1 (en) * | 2002-08-19 | 2006-03-16 | Sang-Mun Jeong | Hydrocarbon steam cracking catalyst for olefin preparation, method for preparing the same, and olefin preparation method using the same |
| US7531706B2 (en) | 2002-10-28 | 2009-05-12 | Idemitsu Kosan Co., Ltd. | Process for producing olefin by catalytic cracking of hydrocarbon |
| US20060116544A1 (en) * | 2002-10-28 | 2006-06-01 | Idemitsu Kosan Co., Ltd. | Process for producing olefin by catalytic cracking of hydrocarbon |
| US20070170093A1 (en) * | 2004-04-22 | 2007-07-26 | Sang-Mun Jeong | Hydrocarbon cracking catalyst and method for preparing the same |
| US20060178546A1 (en) * | 2004-08-10 | 2006-08-10 | Weijian Mo | Method and apparatus for making a middle distillate product and lower olefins from a hydrocarbon feedstock |
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| US20060084568A1 (en) * | 2004-10-18 | 2006-04-20 | Filimonov Igor N | Hydrocarbon cracking catalyst using chemical liquid depositon and method for preparing the same |
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| CN100392047C (en) * | 2005-06-09 | 2008-06-04 | 中国科学院大连化学物理研究所 | A method for producing olefins by catalytic oxidation cracking of petroleum hydrocarbons |
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Also Published As
| Publication number | Publication date |
|---|---|
| BE846507A (en) | 1977-03-23 |
| IT1070567B (en) | 1985-03-29 |
| CA1077067A (en) | 1980-05-06 |
| FR2325711A1 (en) | 1977-04-22 |
| JPS5239604A (en) | 1977-03-28 |
| GB1492880A (en) | 1977-11-23 |
| FR2325711B1 (en) | 1982-08-20 |
| DE2641455A1 (en) | 1977-04-07 |
| NL7610632A (en) | 1977-03-29 |
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